Find important forms to complete for the 2022 RFA Application here:
PHS Human Subjects and Clinical Trials Information
The Human Subjects and Clinical Trials Information form and Study Record form are available below. Please note the documents may display as unavailable when opened in your browser. Please open the PDFs in the Adobe Acrobat desktop application to view and complete them.
Human Subjects and Clinical Trials resources and annotated forms are also available on the NIH website.
Data Safety Monitoring and SO COI Form
The Data Safety Monitoring Plan (DSMP) template is strongly encouraged for applicants to use and can be found below.
Any trial that is more than minimal risk will a safety officer or other independent data and safety monitoring oversight and will need the SO COI Form below completed.
Note that a safety officer has a COI with a project if they’ve published with any key personnel on the project in the past 3 years. The safety officer cannot be a named personnel on the project.
Itemized Budget and Justification
The NIH RR Budget Form can be found below. Please note the document may display as unavailable when opened in your browser. Please open the PDF in the Adobe Acrobat desktop application to view and complete it.
The PHS 394 Form Page 4 and Checklist form can also be used.